AXIV Sinus OVERNIGHT

AXIV Sinus OVERNIGHT is an FDA-registered drug product whose active ingredient is OXYMETAZOLINE HYDROCHLORIDE.. It is labelled by VIVUNT PHARMA LLC taken by nasal and marketed as a human otc drug product. Identifiers on file: NDC 82706-034, application M012, label effective 20260623. It is one of 2 FDA drug label records sharing the active ingredient OXYMETAZOLINE HYDROCHLORIDE.. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing OXYMETAZOLINE HYDROCHLORIDE. are most often described in connection with: temporarily relieves, nasal congestion, due cold, hay fever, upper respiratory, allergies sinus. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses temporarily relieves nasal congestion due to a cold hay fever or other upper respiratory allergies sinus congestion and pressure.

Directions adults and children 6 to under 12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour period. children under 6 years of age: ask a doctor To Use remove protective cap before using for the first time, prime the pump by firmly depressing its rim several times hold container with thumb at base and nozzle between first and second fingers without tilting your head, inset nozzle into nostril fully depress rim with a firm, even stroke and inhale deeply. How to use: Hold white tabs; SQUEEZE grooved area of cap FIRMLY and turn counter clockwise. Secure cap after use. Directions

Warnings Warnings When using this product Do not exceed recommended dosage do not use this product for more than 3 days. Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen. do not use this product if you have heart disease high blood pressure thyroid disease diabetes or difficulty in urination due to enlargement of the prostate gland unless directed by a doctor. this product may cause temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge. use of this comtainer by more than one person may spread infection. Stop use and ask a doctor if symptoms persist. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 2 drug label records with OXYMETAZOLINE HYDROCHLORIDE. as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is AXIV Sinus OVERNIGHT used for?
Uses temporarily relieves nasal congestion due to a cold hay fever or other upper respiratory allergies sinus congestion and pressure.

Who makes AXIV Sinus OVERNIGHT?
VIVUNT PHARMA LLC is the labeler of record for AXIV Sinus OVERNIGHT. 2 FDA label records share the active ingredient OXYMETAZOLINE HYDROCHLORIDE., so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does AXIV Sinus OVERNIGHT come in?
administered by nasal. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is AXIV Sinus OVERNIGHT prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing OXYMETAZOLINE HYDROCHLORIDE.?
Yes. 2 FDA drug label records list OXYMETAZOLINE HYDROCHLORIDE. as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has AXIV Sinus OVERNIGHT been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.